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A SARS-CoV-2 variant with the 12-bp deletion at E gene
The coronavirus disease 2019 (COVID-19) pandemic is still ongoing and has become an important public health threat. This disease is caused by a new coronavirus named severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection, and so far, little is known about this virus. In this study, b...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7598948/ https://www.ncbi.nlm.nih.gov/pubmed/33118859 http://dx.doi.org/10.1080/22221751.2020.1837017 |
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author | Sun, Yi-Sheng Xu, Fang An, Qi Chen, Chen Yang, Zhang-Nv Lu, Hang-Jing Chen, Jian-Cai Yao, Ping-Ping Jiang, Jian-Min Zhu, Han-Ping |
author_facet | Sun, Yi-Sheng Xu, Fang An, Qi Chen, Chen Yang, Zhang-Nv Lu, Hang-Jing Chen, Jian-Cai Yao, Ping-Ping Jiang, Jian-Min Zhu, Han-Ping |
author_sort | Sun, Yi-Sheng |
collection | PubMed |
description | The coronavirus disease 2019 (COVID-19) pandemic is still ongoing and has become an important public health threat. This disease is caused by a new coronavirus named severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection, and so far, little is known about this virus. In this study, by using plaque purification, we purified two SARS-CoV-2 virus strains from the same specimen, one named F8 containing a 12-bp deletion in the E gene and the other named 8X containing the wild-type E gene. There was no significant difference in the viral titer and infectivity of these two strains. The S protein content of the F8 viral culture was 0.39 μg/ml, much higher than that of 8X. An inactivated vaccine made from the F8 strain could trigger high levels of the IgG titer and neutralizing antibody titer, which could last for at least 6 weeks and were significantly higher than those from the 8X strain at 1 and 3 weeks post vaccination, respectively. In conclusion, we reported that both the E gene mutant and wild-type SARS-CoV-2 strains were isolated from the same clinical sample by plaque purification. A 12-bp deletion in the E gene was important for SARS-CoV-2 replication and immunogenicity. |
format | Online Article Text |
id | pubmed-7598948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-75989482020-11-12 A SARS-CoV-2 variant with the 12-bp deletion at E gene Sun, Yi-Sheng Xu, Fang An, Qi Chen, Chen Yang, Zhang-Nv Lu, Hang-Jing Chen, Jian-Cai Yao, Ping-Ping Jiang, Jian-Min Zhu, Han-Ping Emerg Microbes Infect Research Article The coronavirus disease 2019 (COVID-19) pandemic is still ongoing and has become an important public health threat. This disease is caused by a new coronavirus named severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection, and so far, little is known about this virus. In this study, by using plaque purification, we purified two SARS-CoV-2 virus strains from the same specimen, one named F8 containing a 12-bp deletion in the E gene and the other named 8X containing the wild-type E gene. There was no significant difference in the viral titer and infectivity of these two strains. The S protein content of the F8 viral culture was 0.39 μg/ml, much higher than that of 8X. An inactivated vaccine made from the F8 strain could trigger high levels of the IgG titer and neutralizing antibody titer, which could last for at least 6 weeks and were significantly higher than those from the 8X strain at 1 and 3 weeks post vaccination, respectively. In conclusion, we reported that both the E gene mutant and wild-type SARS-CoV-2 strains were isolated from the same clinical sample by plaque purification. A 12-bp deletion in the E gene was important for SARS-CoV-2 replication and immunogenicity. Taylor & Francis 2020-10-29 /pmc/articles/PMC7598948/ /pubmed/33118859 http://dx.doi.org/10.1080/22221751.2020.1837017 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sun, Yi-Sheng Xu, Fang An, Qi Chen, Chen Yang, Zhang-Nv Lu, Hang-Jing Chen, Jian-Cai Yao, Ping-Ping Jiang, Jian-Min Zhu, Han-Ping A SARS-CoV-2 variant with the 12-bp deletion at E gene |
title | A SARS-CoV-2 variant with the 12-bp deletion at E gene |
title_full | A SARS-CoV-2 variant with the 12-bp deletion at E gene |
title_fullStr | A SARS-CoV-2 variant with the 12-bp deletion at E gene |
title_full_unstemmed | A SARS-CoV-2 variant with the 12-bp deletion at E gene |
title_short | A SARS-CoV-2 variant with the 12-bp deletion at E gene |
title_sort | sars-cov-2 variant with the 12-bp deletion at e gene |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7598948/ https://www.ncbi.nlm.nih.gov/pubmed/33118859 http://dx.doi.org/10.1080/22221751.2020.1837017 |
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